Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox1 |
T |
A |
11: 116,065,231 (GRCm39) |
D608V |
probably damaging |
Het |
Actg1 |
A |
T |
11: 120,239,013 (GRCm39) |
C26S |
unknown |
Het |
Ahnak |
T |
A |
19: 8,988,247 (GRCm39) |
V3177E |
possibly damaging |
Het |
Akap11 |
G |
A |
14: 78,750,938 (GRCm39) |
T483I |
|
Het |
Akr1cl |
A |
G |
1: 65,063,830 (GRCm39) |
S120P |
probably benign |
Het |
Ankle2 |
G |
A |
5: 110,400,610 (GRCm39) |
V649M |
possibly damaging |
Het |
Ankrd55 |
A |
T |
13: 112,504,570 (GRCm39) |
I439F |
probably damaging |
Het |
Asb8 |
A |
G |
15: 98,040,635 (GRCm39) |
M9T |
possibly damaging |
Het |
Ascc1 |
A |
T |
10: 59,843,645 (GRCm39) |
Y69F |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,518,060 (GRCm39) |
|
probably null |
Het |
Cd8b1 |
T |
C |
6: 71,306,752 (GRCm39) |
F160L |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,818,350 (GRCm39) |
T842A |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,630,847 (GRCm39) |
K552* |
probably null |
Het |
Cntnap4 |
C |
T |
8: 113,602,600 (GRCm39) |
T1227M |
possibly damaging |
Het |
Cobll1 |
C |
A |
2: 64,981,333 (GRCm39) |
V86F |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,255,561 (GRCm39) |
N2419S |
probably damaging |
Het |
Dhx30 |
A |
T |
9: 109,914,494 (GRCm39) |
L1001* |
probably null |
Het |
Diaph1 |
C |
T |
18: 38,024,162 (GRCm39) |
V559M |
unknown |
Het |
Dock7 |
T |
G |
4: 98,877,350 (GRCm39) |
T1063P |
unknown |
Het |
Dsc1 |
T |
C |
18: 20,232,214 (GRCm39) |
T265A |
possibly damaging |
Het |
Eif2ak4 |
A |
T |
2: 118,258,393 (GRCm39) |
Q581L |
probably damaging |
Het |
Eprs1 |
A |
T |
1: 185,106,334 (GRCm39) |
D183V |
possibly damaging |
Het |
Fads2 |
G |
C |
19: 10,069,183 (GRCm39) |
D80E |
probably benign |
Het |
Fam167b |
G |
A |
4: 129,470,875 (GRCm39) |
R158C |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,892,976 (GRCm38) |
I682K |
possibly damaging |
Het |
Garin4 |
G |
A |
1: 190,894,900 (GRCm39) |
T581I |
possibly damaging |
Het |
Gpatch2l |
C |
T |
12: 86,291,152 (GRCm39) |
P112S |
probably benign |
Het |
Gpn1 |
T |
A |
5: 31,654,710 (GRCm39) |
H87Q |
unknown |
Het |
Greb1l |
T |
C |
18: 10,499,983 (GRCm39) |
V350A |
probably benign |
Het |
Grm5 |
A |
T |
7: 87,724,024 (GRCm39) |
K771N |
probably damaging |
Het |
Gucy2c |
C |
T |
6: 136,728,045 (GRCm39) |
S319N |
probably benign |
Het |
H2bc8 |
A |
G |
13: 23,755,761 (GRCm39) |
D52G |
probably damaging |
Het |
Hcfc2 |
G |
T |
10: 82,535,041 (GRCm39) |
A22S |
probably benign |
Het |
Hnf4a |
A |
G |
2: 163,393,497 (GRCm39) |
D39G |
probably benign |
Het |
Il6st |
C |
T |
13: 112,635,340 (GRCm39) |
T584M |
probably damaging |
Het |
Irf3 |
T |
A |
7: 44,650,246 (GRCm39) |
V254E |
possibly damaging |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Kank4 |
T |
A |
4: 98,668,289 (GRCm39) |
K53* |
probably null |
Het |
Kcnj11 |
A |
T |
7: 45,748,176 (GRCm39) |
F382L |
possibly damaging |
Het |
Kcnq3 |
T |
C |
15: 65,867,510 (GRCm39) |
Y711C |
probably damaging |
Het |
Kctd3 |
A |
G |
1: 188,704,636 (GRCm39) |
S712P |
possibly damaging |
Het |
Krt20 |
A |
G |
11: 99,323,087 (GRCm39) |
I245T |
possibly damaging |
Het |
Larp1b |
T |
C |
3: 40,925,039 (GRCm39) |
I219T |
probably damaging |
Het |
Lman2l |
A |
G |
1: 36,478,771 (GRCm39) |
F114L |
probably damaging |
Het |
Loxl2 |
T |
A |
14: 69,929,859 (GRCm39) |
Y746N |
possibly damaging |
Het |
Lrrc43 |
T |
C |
5: 123,646,109 (GRCm39) |
S628P |
probably benign |
Het |
Mroh8 |
A |
C |
2: 157,111,545 (GRCm39) |
D136E |
probably damaging |
Het |
Nek8 |
T |
A |
11: 78,063,342 (GRCm39) |
M141L |
probably benign |
Het |
Nr2e1 |
C |
A |
10: 42,454,268 (GRCm39) |
R22L |
probably damaging |
Het |
Nr6a1 |
C |
T |
2: 38,816,129 (GRCm39) |
|
probably null |
Het |
Onecut2 |
A |
G |
18: 64,473,890 (GRCm39) |
Y147C |
probably damaging |
Het |
Or1ad1 |
T |
A |
11: 50,876,166 (GRCm39) |
C213S |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,214 (GRCm39) |
M297L |
possibly damaging |
Het |
Or5d37 |
A |
G |
2: 87,924,194 (GRCm39) |
F29L |
probably damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,908 (GRCm39) |
M152V |
probably benign |
Het |
Pcdhac2 |
T |
C |
18: 37,277,316 (GRCm39) |
F99L |
probably benign |
Het |
Pcdhga2 |
T |
G |
18: 37,802,795 (GRCm39) |
V213G |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,519,908 (GRCm39) |
V909E |
probably benign |
Het |
Pik3r4 |
A |
T |
9: 105,547,038 (GRCm39) |
T939S |
probably benign |
Het |
Pip4k2c |
T |
C |
10: 127,035,246 (GRCm39) |
D374G |
possibly damaging |
Het |
Plxdc1 |
A |
T |
11: 97,844,788 (GRCm39) |
D252E |
probably benign |
Het |
Pm20d1 |
A |
C |
1: 131,730,115 (GRCm39) |
D218A |
probably damaging |
Het |
Polq |
C |
A |
16: 36,865,265 (GRCm39) |
Q706K |
probably damaging |
Het |
Pram1 |
A |
T |
17: 33,860,131 (GRCm39) |
I233F |
probably benign |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,061,361 (GRCm39) |
H143Q |
probably damaging |
Het |
Ptpn21 |
A |
G |
12: 98,655,261 (GRCm39) |
Y569H |
probably damaging |
Het |
Rad17 |
T |
C |
13: 100,773,564 (GRCm39) |
K142E |
probably damaging |
Het |
Rcan3 |
T |
C |
4: 135,152,607 (GRCm39) |
E38G |
probably benign |
Het |
Rgl3 |
C |
A |
9: 21,885,356 (GRCm39) |
R658L |
possibly damaging |
Het |
Rnf125 |
T |
A |
18: 21,116,240 (GRCm39) |
*141K |
probably null |
Het |
Ros1 |
G |
T |
10: 52,019,502 (GRCm39) |
N711K |
probably damaging |
Het |
Rsph10b |
T |
A |
5: 143,896,504 (GRCm39) |
Y421N |
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,776,471 (GRCm39) |
V2222I |
probably damaging |
Het |
Samsn1 |
C |
T |
16: 75,656,449 (GRCm39) |
C333Y |
probably damaging |
Het |
Slc9a2 |
G |
A |
1: 40,794,944 (GRCm39) |
E502K |
probably benign |
Het |
Stard9 |
A |
T |
2: 120,533,500 (GRCm39) |
E3252D |
possibly damaging |
Het |
Syne1 |
C |
A |
10: 5,123,008 (GRCm39) |
R309S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,172,289 (GRCm39) |
I5051V |
probably benign |
Het |
Syngap1 |
A |
G |
17: 27,183,948 (GRCm39) |
S1241G |
probably damaging |
Het |
Tbpl2 |
T |
C |
2: 23,966,030 (GRCm39) |
K321R |
probably damaging |
Het |
Tnrc18 |
C |
T |
5: 142,717,107 (GRCm39) |
G2449E |
probably damaging |
Het |
Trim25 |
A |
G |
11: 88,901,731 (GRCm39) |
D342G |
probably benign |
Het |
Tssk4 |
T |
A |
14: 55,887,904 (GRCm39) |
H33Q |
probably benign |
Het |
Ttc3 |
G |
A |
16: 94,268,831 (GRCm39) |
G1971D |
possibly damaging |
Het |
Tufm |
C |
T |
7: 126,088,849 (GRCm39) |
Q347* |
probably null |
Het |
Ubxn10 |
G |
A |
4: 138,448,133 (GRCm39) |
S181F |
possibly damaging |
Het |
Ushbp1 |
T |
C |
8: 71,841,539 (GRCm39) |
E430G |
probably benign |
Het |
Vmn1r33 |
T |
C |
6: 66,588,716 (GRCm39) |
I279M |
possibly damaging |
Het |
Vmn2r115 |
T |
C |
17: 23,564,784 (GRCm39) |
F224L |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,681,323 (GRCm39) |
H77L |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,663,961 (GRCm39) |
I1481V |
probably benign |
Het |
Vps35 |
T |
C |
8: 86,007,898 (GRCm39) |
N294S |
possibly damaging |
Het |
Washc3 |
A |
T |
10: 88,051,916 (GRCm39) |
T102S |
probably benign |
Het |
Zfp27 |
T |
A |
7: 29,595,359 (GRCm39) |
E202V |
possibly damaging |
Het |
Zfp58 |
T |
C |
13: 67,640,035 (GRCm39) |
H152R |
possibly damaging |
Het |
Zfr2 |
T |
C |
10: 81,080,496 (GRCm39) |
V390A |
probably damaging |
Het |
|
Other mutations in Dis3l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01736:Dis3l
|
APN |
9 |
64,226,536 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01812:Dis3l
|
APN |
9 |
64,217,519 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01838:Dis3l
|
APN |
9 |
64,215,581 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02104:Dis3l
|
APN |
9 |
64,217,611 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02478:Dis3l
|
APN |
9 |
64,222,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02481:Dis3l
|
APN |
9 |
64,226,362 (GRCm39) |
splice site |
probably null |
|
IGL02483:Dis3l
|
APN |
9 |
64,226,362 (GRCm39) |
splice site |
probably null |
|
IGL02965:Dis3l
|
APN |
9 |
64,217,766 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03139:Dis3l
|
APN |
9 |
64,219,232 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03054:Dis3l
|
UTSW |
9 |
64,217,722 (GRCm39) |
critical splice donor site |
probably null |
|
R0066:Dis3l
|
UTSW |
9 |
64,226,447 (GRCm39) |
missense |
probably benign |
0.27 |
R0066:Dis3l
|
UTSW |
9 |
64,226,447 (GRCm39) |
missense |
probably benign |
0.27 |
R0724:Dis3l
|
UTSW |
9 |
64,214,408 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0801:Dis3l
|
UTSW |
9 |
64,226,436 (GRCm39) |
missense |
probably benign |
|
R0925:Dis3l
|
UTSW |
9 |
64,248,412 (GRCm39) |
start codon destroyed |
probably null |
0.97 |
R1502:Dis3l
|
UTSW |
9 |
64,233,069 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1541:Dis3l
|
UTSW |
9 |
64,214,771 (GRCm39) |
missense |
probably benign |
0.07 |
R1794:Dis3l
|
UTSW |
9 |
64,225,058 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1929:Dis3l
|
UTSW |
9 |
64,238,165 (GRCm39) |
missense |
probably damaging |
0.96 |
R2007:Dis3l
|
UTSW |
9 |
64,215,558 (GRCm39) |
splice site |
probably null |
|
R2062:Dis3l
|
UTSW |
9 |
64,246,855 (GRCm39) |
missense |
probably benign |
0.02 |
R2152:Dis3l
|
UTSW |
9 |
64,214,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2153:Dis3l
|
UTSW |
9 |
64,214,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2154:Dis3l
|
UTSW |
9 |
64,214,545 (GRCm39) |
missense |
probably benign |
0.00 |
R2186:Dis3l
|
UTSW |
9 |
64,246,894 (GRCm39) |
nonsense |
probably null |
|
R2271:Dis3l
|
UTSW |
9 |
64,238,165 (GRCm39) |
missense |
probably damaging |
0.96 |
R2280:Dis3l
|
UTSW |
9 |
64,225,076 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2287:Dis3l
|
UTSW |
9 |
64,214,779 (GRCm39) |
missense |
probably benign |
0.20 |
R3156:Dis3l
|
UTSW |
9 |
64,219,032 (GRCm39) |
missense |
probably benign |
0.25 |
R4664:Dis3l
|
UTSW |
9 |
64,238,080 (GRCm39) |
missense |
unknown |
|
R4775:Dis3l
|
UTSW |
9 |
64,238,190 (GRCm39) |
missense |
probably benign |
0.16 |
R4977:Dis3l
|
UTSW |
9 |
64,214,483 (GRCm39) |
missense |
probably benign |
0.00 |
R4997:Dis3l
|
UTSW |
9 |
64,219,224 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5097:Dis3l
|
UTSW |
9 |
64,226,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R5579:Dis3l
|
UTSW |
9 |
64,238,117 (GRCm39) |
missense |
probably benign |
0.44 |
R5623:Dis3l
|
UTSW |
9 |
64,214,885 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6310:Dis3l
|
UTSW |
9 |
64,229,857 (GRCm39) |
missense |
probably benign |
0.00 |
R6442:Dis3l
|
UTSW |
9 |
64,214,837 (GRCm39) |
missense |
probably benign |
|
R6505:Dis3l
|
UTSW |
9 |
64,214,795 (GRCm39) |
missense |
probably benign |
0.15 |
R6731:Dis3l
|
UTSW |
9 |
64,217,720 (GRCm39) |
splice site |
probably null |
|
R7008:Dis3l
|
UTSW |
9 |
64,217,735 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7405:Dis3l
|
UTSW |
9 |
64,221,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Dis3l
|
UTSW |
9 |
64,219,219 (GRCm39) |
nonsense |
probably null |
|
R7798:Dis3l
|
UTSW |
9 |
64,248,299 (GRCm39) |
missense |
probably benign |
|
R7890:Dis3l
|
UTSW |
9 |
64,229,753 (GRCm39) |
missense |
probably benign |
0.00 |
R8329:Dis3l
|
UTSW |
9 |
64,219,112 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8715:Dis3l
|
UTSW |
9 |
64,214,342 (GRCm39) |
missense |
probably benign |
|
R8942:Dis3l
|
UTSW |
9 |
64,214,875 (GRCm39) |
missense |
probably benign |
0.22 |
R8973:Dis3l
|
UTSW |
9 |
64,246,824 (GRCm39) |
missense |
probably damaging |
0.96 |
R9240:Dis3l
|
UTSW |
9 |
64,217,447 (GRCm39) |
critical splice donor site |
probably null |
|
R9354:Dis3l
|
UTSW |
9 |
64,221,922 (GRCm39) |
missense |
probably benign |
0.01 |
R9394:Dis3l
|
UTSW |
9 |
64,225,017 (GRCm39) |
missense |
probably benign |
0.24 |
R9569:Dis3l
|
UTSW |
9 |
64,236,829 (GRCm39) |
missense |
unknown |
|
X0020:Dis3l
|
UTSW |
9 |
64,233,016 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Dis3l
|
UTSW |
9 |
64,214,336 (GRCm39) |
missense |
probably damaging |
0.99 |
|